408352-48-7 Usage
Uses
Used in Pharmaceutical and Agrochemical Industries:
4,6-dibromopyridin-2-amine is used as a key intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its unique structure allows for the development of new compounds with specific therapeutic or pesticidal properties, contributing to advancements in these industries.
Used in Organic Synthesis:
4,6-dibroMopyridin-2-aMine serves as a valuable building block in the preparation of heterocyclic compounds and other organic synthesis applications. Its reactivity and functional groups make it suitable for a wide range of chemical reactions, enabling the creation of diverse molecules with potential applications in various fields.
Used in Material Science:
4,6-dibromopyridin-2-amine has potential use as a building block in material science, particularly in the development of specialty polymers or functionalized materials. Its unique structure and properties can be leveraged to create new materials with specific characteristics, such as improved mechanical strength, thermal stability, or chemical resistance.
Safety Precautions:
It is important to handle 4,6-dibromopyridin-2-amine with care, as it is a potentially hazardous chemical. Proper safety protocols should be followed during its use, storage, and disposal to minimize risks to human health and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 408352-48-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,8,3,5 and 2 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 408352-48:
(8*4)+(7*0)+(6*8)+(5*3)+(4*5)+(3*2)+(2*4)+(1*8)=137
137 % 10 = 7
So 408352-48-7 is a valid CAS Registry Number.
408352-48-7Relevant academic research and scientific papers
Bromation regioselective en serie aromatique. I: Monobromation en position para de phenols et d'amines aromatiques par le tribromure de tetrabutylammonium
Berthelot, Jacques,Guette, Catherine,Desbene, Paul-Louis,Basselier, Jean-Jacques,Chaquin, Patrick,Masure, Daniel
, p. 2061 - 2066 (2007/10/02)
The reaction of tetrabutylammonium tribromide (TBABr3) with phenols and aromatic amines in aprotic and non-basic solvents at 20 deg C gives exclusively the corresponding para-brominated compounds in high yields.A mechanism involving electrophilic substitution by the tribromide anion Br3- itself is suggested to account for the results, especially the regioselective para bromination.Key words: bromination, tetrabutylammonium tribromide, phenols, aromatic amines.
